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DO Term : autosomal dominant beta thalassemia [DOID:0080770] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A beta thalassemia that has_material_basis_in one dominantly inherited mutated HBB gene and signs and symptoms of beta-thalassemia major or beta-thalassemia intermedia.

synonyms:
OMIM:603902,
inclusion body beta-thalassemia,
603902

Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents

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